Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 11:25 PM
Ignite Modification Date:
2025-12-25 @ 9:11 PM
NCT ID:
NCT01371656
Group ID:
EG000
Title:
Arm I (Levofloxacin)
Description:
Patients receive levofloxacin PO or IV over 60-90 minutes once or twice daily beginning on day 3 during 2 consecutive courses of chemotherapy or beginning on day -2 during HSCT and continuing until blood counts recover.
levofloxacin: Given PO or IV
Deaths Number Affected:
69
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
306
Other Number Affected:
36
Other Number At Risk:
306
Study:
NCT01371656
Results Section:
NCT01371656
Adverse Events Module:
NCT01371656